Package 50268-685-15

Brand: prochlorperazine maleate

Generic: prochlorperazine maleate
NDC Package

Package Facts

Identity

Package NDC 50268-685-15
Digits Only 5026868515
Product NDC 50268-685
Product ID 50268-685_423994fe-6cd5-476d-e063-6294a90a5814
Description

50 BLISTER PACK in 1 BOX (50268-685-15) / 1 TABLET in 1 BLISTER PACK (50268-685-11)

Marketing

Marketing Status
Marketed Since 2019-04-16
Brand prochlorperazine maleate
Generic prochlorperazine maleate
Sample Package No

Linked Drug Pages (1)

PROCHLORPERAZINE MALEATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "423994fe-6cd5-476d-e063-6294a90a5814", "openfda": {"unii": ["I1T8O1JTL6"], "rxcui": ["198365", "312635"], "spl_set_id": ["86ac7223-b840-bc0c-e053-2991aa0a32f2"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-685-15)  / 1 TABLET in 1 BLISTER PACK (50268-685-11)", "package_ndc": "50268-685-15", "marketing_start_date": "20190416"}], "brand_name": "PROCHLORPERAZINE MALEATE", "product_id": "50268-685_423994fe-6cd5-476d-e063-6294a90a5814", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "50268-685", "generic_name": "Prochlorperazine maleate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROCHLORPERAZINE MALEATE", "active_ingredients": [{"name": "PROCHLORPERAZINE MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA040268", "marketing_category": "ANDA", "marketing_start_date": "20190416", "listing_expiration_date": "20261231"}